bicentennial
Senior Member (Voting Rights)
I did not know it had been referred to the Law Commission. Have you any links?
I think that NICE, the Family Court, NHS England, and the Children's Commissioner should have told you in reply to your letter. Or at least passed on your letter, since they do prioritise safeguarding. After all, you could have been consulted on this legal reform, and as you said:
... there is no excuse for ignorance in the Law
Thankyou @Tilly and @Maat. You posted in August 2025.
The Final Delivery Plan for ME/CFS was published on 25 July 2025, as a Policy Paper for the Departments of Education, Work & Pensions, also Health & Social Care.
The IDP [Interim Delivery Plan?] had agreed [when?] that:
the Law Commission will review existing social care legislation relating to disabled children, to improve clarity for families about the support that they are legally entitled to, ensuring that local authorities know what they are expected to provide, and families know how to access support
Did this review happen yet? Is it published, or is it not yet presentable? What were the local authorities told to provide for? Do families now know how to access what?
DHSC will engage stakeholders to discuss timely diagnosis and support for children who have ME/CFS and their families as well as best practice in relation to safeguarding responsibilities
Oh good. Maybe the DHSC already had a definition from the Law Commission.
Where is the best safeguarding practice defined? Apart from the definitive NICE Recommendation on ME/CFS Safeguarding, and the BASW procedure for suspected FII Safeguarding. Because no stakeholder dared present confidential safeguarding definitions to NICE. Not for the asking. Only children, families and carers dared
In the consultation, 98.5% of respondents selected ‘strongly agree’ or ‘agree’ to the contents outlined in the ‘Support for children and young people with ME/CFS’ section of the IDP.
Nice. We got most of the targeted minors theoretically helped. Are there signs that this was delivered in practice?
However, respondents made suggestions on where we could improve actions, particularly regarding:
- the pressure and harm of physical attendance
- improving awareness to prevent harm from false accusation of fabricated illness
- adaptations to physical environments and integration of pacing to support education
- the need for education and recognition of ME/CFS as a disability to improve access to support in schools
- the difficulty accessing timely support for children
- financial pressures for families and support for adapting education
The Law Commission DID examine the evidence, and made its Recommendations already. Parliament held out a bit longer for some autism report. But the French are being pointed at us in the UK, now, by some French eejit trashing our health and safety criteria as determined by NICE. Apparently we deluded our government too, lol.
As such, in addition to the actions agreed in the IDP, we have agreed that DfE will embed ME/CFS-specific considerations into its broader approach to education, including by sharing relevant training, resources and guidance with alternative provision settings and local authorities.
In addition, DfE will explore opportunities to raise awareness and promote understanding of ME/CFS across the education sector. This includes engaging with stakeholders, disseminating best practice, and ensuring that guidance and communications reflect the needs of children with complex medical conditions.
So are children still being persecuted or did it all stop? Did disabled parents get a new report to update on the Jigsaw Report? Did the Social Workers relent when assessing provision for Community Care, and for Children and Families? Did they start to reveal and offer the liberating personal budgets, as directed (since 2010).
Also, there are clauses for disabled children in the new law recommendations that should apply to all children. And - due to some hair-raising reports - I want to see protections for children being confidentially researched by enforcing doctors.
Safe-guarding service networks were too confused to be safe, so they only need to read the NICE Guideline. But when a safe-guarder lies it is with malice aforethought.
Attached file is the
Impact Assessment for the Final Report on Disabled Children's Social Care
Attachments
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